A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570059



Internal ID20943130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16477980..16478370hg38UCSC Ensembl
chr7:16517605..16517995hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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